A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106809



Internal ID20673849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100141995..100147531hg38UCSC Ensembl
chr4:101063152..101068688hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg385537
hg195537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392233
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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